US8658835B2

US8658835B2 - Oxidation of hydrocarbons

Info

Publication number: US8658835B2
Application number: US13/386,250
Authority: US
Inventors: Kun Wang; Jihad M. Dakka; Stephen Zushma
Original assignee: ExxonMobil Chemical Patents Inc
Current assignee: ExxonMobil Chemical Patents Inc
Priority date: 2007-10-31
Filing date: 2010-07-13
Publication date: 2014-02-25
Anticipated expiration: 2028-10-08
Also published as: CN102482211A; WO2011031374A2; WO2011031374A3; EP2470501A2; SG178202A1; US20120149941A1; CN106117099A

Abstract

In a process for oxidizing a hydrocarbon to a corresponding hydroperoxide, alcohol, ketone, carboxylic acid or dicarboxylic acid, the hydrocarbon is contacted with an oxygen-containing gas in the presence of a catalyst comprising a cyclic imide. The contacting produces an effluent comprising an oxidized hydrocarbon product and unreacted imide catalyst and the effluent is treated with at least one solid sorbent to remove at least part of the unreacted imide catalyst and produce a treated effluent comprising said oxidized hydrocarbon product. The organic phase can then be recovered.

Description

PRIORITY CLAIM

This application is a national Stage Application of International Application No. PCT/US2010/041801 filed Jul. 13, 2010, which claims the benefit of prior U.S. provisional application Ser. No. 61/237,983 filed Aug. 28, 2009, both of which are hereby incorporated by reference in their entirety. The present application is also a continuation-in-part application of U.S. patent application Ser. No. 12/675,342 entitled “Oxidation of Hydrocarbons,” which is the U.S. national phase application of PCT/US2008/079150 entitled “Oxidation of Hydrocarbons,” which has an international filing date of Oct. 8, 2008 and claims priority to U.S. provisional application Ser. No. 60/984,264, which, in turn, was filed on Oct. 31, 2007 and entitled “Oxidation of Hydrocarbons,” the contents of all of which are hereby incorporated by reference in their entirety.

FIELD OF THE INVENTION

The present invention relates to a process for oxidizing hydrocarbons and, in particular, alkylaromatic hydrocarbons to produce for example phenol and substituted phenols.

BACKGROUND OF THE INVENTION

The oxidation of hydrocarbons is an important reaction in industrial organic chemistry. Thus, for example, the oxidation of cyclohexane is used commercially to produce cyclohexanol and cyclohexanone, which are important precursors in the production of nylon, whereas oxidation of alkylaromatic hydrocarbons is used to produce phenol, a precursor in the production of polycarbonates and epoxy resins.

Oxidation of hydrocarbons can be conducted using well-known oxidizing agents, such as KMnO₄, CrO₃and HNO₃. However, these oxidizing agents have the disadvantage of being relatively expensive, and moreover their use is accompanied by the production of unwanted coupling products which can represent disposal problems and ecological pollution.

Preferably, therefore, oxidizing agents based on peroxides or N₂O are used. The cheapest oxidizing agent, however, is molecular oxygen, either in pure form or as atmospheric oxygen. However, oxygen itself is usually unsuitable for oxidizing hydrocarbons, since the reactivity of the O₂molecule, which occurs in the energetically favorable triplet form, is not sufficient.

By using redox metal catalysts it is possible to utilize molecular oxygen for oxidizing organic compounds and hence a great number of industrial processes are based on the metal-catalyzed autooxidation of hydrocarbons. Thus, for example, the oxidation of cyclohexane with O₂to cyclohexanol and/or cyclohexanone proceeds with the use of cobalt salts. These industrial processes are based on a free-radical chain mechanism, in which the bi-radical oxygen reacts with a hydrocarbon free radical, with formation of a peroxy radical and subsequent chain propagation by abstraction of an H atom from a further hydrocarbon. In addition to metal salts, however, organic molecules can also act as free-radical initiators.

However, it is a disadvantage of these processes that the selectivity decreases very greatly with increasing conversion and therefore the processes must be operated at a very low level of conversion. Thus, for example, the oxidation of cyclohexane to cyclohexanol/cyclohexanone is carried out at a conversion of 10 to 12% so that the selectivity is 80 to 85% (“Industrielle Organische Chemie” [Industrial Organic Chemistry] 1994, 261, VCH-Verlag, D-69451 Weinheim).

An alternative to metal salt catalysts is the use of organic mediators, for example N-hydroxyphthalimide (NHPI). Thus, U.S. Pat. Nos. 6,852,893 and 6,720,462 describe methods for oxidizing hydrocarbon substrates by contacting the substrate with an oxygen-containing gas, in which the oxygen content is from 5 to 100% by volume, in the presence of a free radical initiator and a catalyst, typically a N-hydroxycarbodiimide catalyst, such as N-hydroxyphthalimide (NHPI). The process is conducted at a temperature between 0° C. and 500° C. and a pressure between atmospheric and 100 bar (100 and 10,000 kPa). The molar ratio of the catalyst to the hydrocarbon substrate can range from 10⁻⁶mol % to 1 mol %, whereas the molar ratio of free-radical initiator to the catalyst can be 4:1 or less, such as 1:1 to 0.5:1. Suitable substrates that may be oxidized by this process include cumene, cyclohexylbenzene, cyclododecylbenzene and sec-butylbenzene.

U.S. Pat. No. 7,038,089 discloses a process for preparing a hydroperoxide from a hydrocarbon selected from a group consisting of primary hydrocarbons, secondary hydrocarbons and mixtures thereof corresponding to said hydroperoxide which comprises conducting oxidation of said hydrocarbon at a temperature in the range between 130 and 160° C. with an oxygen-containing gas in a reaction mixture containing said hydrocarbon and a catalyst comprising a cyclic imide compound and an alkali metal compound. Suitable hydrocarbons are said to include C₄to C₂₀tertiary alkanes (e.g., iso-butane, iso-pentane, iso-hexane, and the like), C₇to C₂₀(alkyl) aromatic hydrocarbons with 1 to 6 aromatic rings or C₉to C₂₀(cycloalkyl) aromatic hydrocarbons with 1 to 6 aromatic rings (e.g., xylene, cumene, cymene, ethylbenzene, diisopropylbenzene, cyclohexylbenzene, tetrahydronaphthalene (tetraline), indane, etc.), and the like. The amount of the cyclic imide compound used may be from 0.0001 to 1%, preferably from 0.0005 to 0.5%, by weight based on the reaction mixture, whereas the amount of the alkali metal compound may be from 0.000005 to 0.01%, preferably from 0.00001 to 0.005%, by weight based on the reaction mixture.

However, although current work has continued to demonstrate the utility of cyclic imides as hydrocarbon oxidation catalysts, it has also shown that their application in a commercial process requires further investigation. In particular, cyclic imides, such as N-hydroxyphthalimide, are expensive and are readily hydrolyzed under the conditions of the oxidation reaction. Moreover, unreacted imide catalysts and their decomposition products (acids and ethers) can pose significant problems to the downstream reactions, such as hydroperoxide cleavage. Thus the successful application of cyclic imides to the oxidation of hydrocarbons requires treatment of the oxidation effluent to remove unreacted imides and their decomposition products and, if possible, recovery and recycle of the valuable unreacted imides.

According to the invention, it has now been found that unreacted imide catalyst and its decomposition products can be at least partially removed from the effluent of the catalytic oxidation of alkylaromatic compounds by treatment of the effluent with at least one solid sorbent chosen from alkali metal carbonates, alkali metal bicarbonates, alkali metal hydroxides, alkali metal hydroxide-carbonate complexes, alkaline earth metal carbonates, alkaline earth metal bicarbonates, alkaline earth metal hydroxides and alkaline earth metal hydroxide-carbonate complexes. The unreacted imide is selectively removed from the effluent leaving a product that is essentially free of the imide species. By subsequently washing the adsorbent with a polar solvent, the imide species can be recovered for recycle to the oxidation step.

SUMMARY OF THE INVENTION

In one aspect, the present invention resides in a process for oxidizing a hydrocarbon to a corresponding hydroperoxide, alcohol, ketone, carboxylic acid or dicarboxylic acid, the process comprising:

(a) contacting a hydrocarbon with an oxygen-containing gas in the presence of a catalyst comprising a cyclic imide of the general formula (I):

wherein each of R¹and R²is independently selected from hydrocarbyl and substituted hydrocarbyl radicals having 1 to 20 carbon atoms, or from the groups SO₃H, NH₂, OH and NO₂, or from the atoms H, F, Cl, Br and I, provided that R¹and R²can be linked to one another via a covalent bond;
each of Q¹and Q²is independently selected from C, CH, N and CR³;
each of X and Z is independently selected from C, S, CH₂, N, P and elements of Group 4 of the Periodic Table;
Y is O or OH;
k is 0, 1, or 2;
l is 0, 1, or 2,
m is 1 to 3; and
R³can be any of the entities (radicals, groups, or atoms) listed for R¹; and wherein said contacting produces an effluent comprising an oxidized hydrocarbon product and unreacted imide catalyst of said formula (I); and

(b) treating the effluent with at least one solid sorbent to remove at least part of said unreacted imide catalyst of said formula (I) from said effluent and produce a treated effluent comprising said oxidized hydrocarbon product.

Conveniently, said at least one solid sorbent is chosen from alkali metal carbonates, alkali metal bicarbonates, alkali metal hydroxides, alkali metal hydroxide-carbonate complexes, alkaline earth metal carbonates, alkaline earth metal bicarbonates, alkaline earth metal hydroxides and alkaline earth metal hydroxide-carbonate complexes.

In one embodiment, the process further comprises recovering the unreacted imide catalyst removed by said at least one solid sorbent and recycling the catalyst to (a). Conveniently, the unreacted imide catalyst is recovered from said at least one solid sorbent by washing the at least one solid sorbent with a polar solvent.

Conveniently, said hydrocarbon is an alkane or cycloalkane, such as isobutane or cyclohexane.

Alternatively, said hydrocarbon is an alkylaromatic compound of general formula (II):

wherein R⁴and R⁵each independently represents hydrogen or an alkyl group having from 1 to 4 carbon atoms, provided that R⁴and R⁵may be joined to form a cyclic group having from 4 to 10 carbon atoms, said cyclic group being optionally substituted, and R⁶represents hydrogen, one or more alkyl groups having from 1 to 4 carbon atoms or a cyclohexyl group.

Conveniently, said alkylaromatic compound of general formula (II) is selected from ethyl benzene, cumene, sec-butylbenzene, sec-pentylbenzene, p-methyl-sec-butylbenzene, 1,4-diphenylcyclohexane, sec-hexylbenzene, and cyclohexylbenzene.

Conveniently, said cyclic imide obeys the general formula (III):

wherein each of R⁷, R⁸, R⁹, and R¹⁰is independently selected from hydrocarbyl and substituted hydrocarbyl radicals having 1 to 20 carbon atoms, or from the groups SO₃H, NH₂, OH and NO₂, or from the atoms H, F, Cl, Br and I;
each of X and Z is independently selected from C, S, CH₂, N, P and an element of Group 4 of the Periodic Table;
Y is O or OH;
k is 0, 1, or 2; and
l is 0, 1, or 2.

In one embodiment, said cyclic imide comprises N-hydroxyphthalimide.

In a further aspect, the present invention resides in a process for producing a phenol, said process comprising:

(a) contacting a reaction medium comprising an alkylaromatic compound of general formula (II):

wherein R⁴and R⁵each independently represents hydrogen or an alkyl group having from 1 to 4 carbon atoms, provided that R⁴and R⁵may be joined to form a cyclic group having from 4 to 10 carbon atoms, said cyclic group being optionally substituted, and R⁶represents hydrogen, one or more alkyl groups having from 1 to 4 carbon atoms or a cyclohexyl group, with oxygen in the presence of a catalyst comprising a cyclic imide of the general formula (I):

wherein each of R¹and R²is independently selected from hydrocarbyl and substituted hydrocarbyl radicals having 1 to 20 carbon atoms, or from the groups SO₃H, NH₂, OH and NO₂, or from the atoms H, F, Cl, Br and I, provided that R¹and R²can be linked to one another via a covalent bond;
each of Q¹and Q²is independently selected from C, CH, N and CR³;
each of X and Z is independently selected from C, S, CH₂, N, P and elements of Group 4 of the Periodic Table;
Y is O or OH;
k is 0, 1, or 2;
l is 0, 1, or 2;
m is 1 to 3; and
R³can be any of the entities (radicals, groups, or atoms) listed for R¹;
wherein said contacting produces an effluent comprising unreacted imide catalyst of said formula (I) and a hydroperoxide of general formula (IV):

in which R⁴, R⁵and R⁶have the same meaning as in formula (II);

(b) treating the effluent with at least one solid sorbent chosen from alkali metal carbonates, alkali metal bicarbonates, alkali metal hydroxides, alkali metal hydroxide-carbonate complexes, alkaline earth metal carbonates, alkaline earth metal bicarbonates, alkaline earth metal hydroxides and alkaline earth metal hydroxide-carbonate complexes to remove at least part of said unreacted imide catalyst of said formula (I) from said effluent and produce a treated effluent comprising said hydroperoxide of general formula (IV); and

(c) converting the hydroperoxide of formula (IV) from said organic phase into a phenol and an aldehyde or ketone of the general formula R⁴COCH₂R⁵(V), in which R⁴and R⁵have the same meaning as in formula (II).

Conveniently, said contacting (a) is conducted at a temperature of between about 20° C. and about 150° C., such as between about 70° C. and about 130° C. The pressure at which the contacting (a) is conducted is conveniently between about 15 kPa and about 500 kPa, such as between 100 kPa to about 150 kPa.

DETAILED DESCRIPTION OF THE EMBODIMENTS

The terms “group”, “radical”, and “substituent” are used interchangeably in this document. For purposes of this disclosure, “hydrocarbyl radical” is defined to be a radical, which contains hydrogen atoms and up to 20 carbon atoms and which may be linear, branched, or cyclic, and when cyclic, aromatic or non-aromatic. “Substituted hydrocarbyl radicals” are radicals in which at least one hydrogen atom in a hydrocarbyl radical has been substituted with at least one functional group or where at least one non-hydrocarbon atom or group has been inserted within the hydrocarbyl radical. Conveniently, each of R¹and R²is independently selected from aliphatic alkoxy or aromatic alkoxy radicals, carboxy radicals, alkoxy-carbonyl radicals and hydrocarbon radicals, each of which radicals has H₀20 carbon atoms.

The present invention provides a process for oxidizing a hydrocarbon to at least one of the corresponding hydroperoxide, alcohol, ketone, carboxylic acid or dicarboxylic acid. The process comprises contacting a reaction medium comprising a hydrocarbon with an oxygen-containing gas in the presence of a catalyst comprising a cyclic imide of the general formula (I):

wherein each of R¹and R²is independently selected from hydrocarbyl and substituted hydrocarbyl radicals having 1 to 20 carbon atoms, or the groups SO₃H, NH₂, OH and NO₂, or the atoms H, F, Cl, Br and I, provided that R¹and R²can be linked to one another via a covalent bond; each of Q¹and Q²is independently selected from C, CH, N and CR³; each of X and Z is independently selected from C, S, CH₂, N, P and elements of Group 4 of the Periodic Table; Y is O or OH; k is 0, 1, or 2; l is 0, 1, or 2; m is 1 to 3; and R³can be any of the entities (radicals, groups, or atoms) listed for R¹. As used herein, the new numbering scheme for the Periodic Table Groups are employed as disclosed in Chemical and Engineering News, 63(5), 27 (1985).

The contacting produces an effluent comprising the desired oxidized hydrocarbon product together with unreacted imide catalyst of said formula (I). The effluent is then treated, before or after concentration of the oxidized hydrocarbon product, with at least one solid sorbent chosen from alkali metal carbonates, alkali metal bicarbonates, alkali metal hydroxides, alkali metal hydroxide-carbonate complexes, alkaline earth metal carbonates, alkaline earth metal bicarbonates, alkaline earth metal hydroxides and alkaline earth metal hydroxide-carbonate complexes so as to remove at least part, and typically to remove substantially all, of said unreacted imide catalyst from the effluent and produce a treated effluent comprising the oxidized hydrocarbon product. The oxidized hydrocarbon product can then be recovered for further processing.

By washing the imide-loaded at least one solid sorbent with a polar solvent, such as ethanol, the unreacted imide catalyst can be recovered for possible recycle to the oxidation step.

Hydrocarbon Feed

Using the present process a wide group of substituted or unsubstituted saturated or unsaturated hydrocarbons, such as alkanes, cycloalkanes, alkenes, cycloalkenes, and aromatics, can be selectively oxidized. In particular, however, the process has utility in the selective oxidation of isobutane to tertiary butyl hydroperoxide and tertiary butanol, the selective oxidation of cyclohexane to cyclohexyl hydroperoxide, cyclohexanol and cyclohexanone and the selective oxidation to the corresponding hydroperoxides of alkylaromatic compounds of the general formula (II):

in which R⁴and R⁵each independently represents hydrogen or an alkyl group having from 1 to 4 carbon atoms, provided that R⁴and R⁵may be joined to form a cyclic group having from 4 to 10 carbon atoms, said cyclic group being optionally substituted, and R⁶represents hydrogen, one or more alkyl groups having from 1 to 4 carbon atoms or a cyclohexyl group. In an embodiment, R⁴and R⁵are joined to form a cyclic group having from 4 to 10 carbon atoms, conveniently a cyclohexyl group, substituted with one or more alkyl group having from 1 to 4 carbon atoms or with one or more phenyl groups. Examples of suitable alkylaromatic compounds are ethyl benzene, cumene, sec-butylbenzene, sec-pentylbenzene, p-methyl-sec-butylbenzene, 1,4-diphenylcyclohexane, sec-hexylbenzene, and cyclohexylbenzene, with sec-butylbenzene and cyclohexylbenzene being preferred. It will also be understood that in the case where R⁴and R⁵are joined to form a cyclic group, the number of carbons forming the cyclic ring is from 4 to 10. However, that ring may itself carry one or more substituents, such as one or more alkyl groups having from 1 to 4 carbon atoms or one or more phenyl groups, as in the case of 1,4-diphenylcyclohexane.

In one practical embodiment, the alkylaromatic compound of general formula (II) is sec-butylbenzene and is produced by alkylating benzene with at least one C₄alkylating agent under alkylation conditions and in the presence of a heterogeneous catalyst, such as zeolite Beta or more preferably at least one molecular sieve of the MCM-22 family (as defined below). The alkylation conditions conveniently include a temperature of from about 60° C. to about 260° C., for example between about 100° C. and about 200° C. The alkylation pressure is conveniently 7000 kPa or less, for example from about 1000 to about 3500 kPa. The alkylation is conveniently carried out at a weight hourly space velocity (WHSV) based on C₄alkylating agent of between about 0.1 and about 50 hr⁻¹, for example between about 1 and about 10 hr⁻¹.

The C₄alkylating agent conveniently comprises at least one linear butene, namely butene-1, butene-2 or a mixture thereof. The alkylating agent can also be an olefinic C₄hydrocarbon mixture containing linear butenes, such as can be obtained by steam cracking of ethane, propane, butane, LPG and light naphthas, catalytic cracking of naphthas and other refinery feedstocks and by conversion of oxygenates, such as methanol, to lower olefins. For example, the following C₄hydrocarbon mixtures are generally available in any refinery employing steam cracking to produce olefins and are suitable for use as the C₄alkylating agent: a crude steam cracked butene stream, Raffinate-1 (the product remaining after solvent extraction or hydrogenation to remove butadiene from the crude steam cracked butene stream) and Raffinate-2 (the product remaining after removal of butadiene and isobutene from the crude steam cracked butene stream).

In a further practical embodiment, the alkylaromatic compound of general formula (II) is cyclohexylbenzene and is produced by contacting benzene with hydrogen in the presence of a heterogeneous bifunctional catalyst which comprises at least one metal having hydrogenation activity, typically selected from the group consisting of palladium, ruthenium, nickel and cobalt, and a crystalline inorganic oxide material having alkylation activity, typically at least one molecular sieve of the MCM-22 family (as defined below). The contacting step is conveniently conducted at a temperature of about 50° C. to about 350° C. The contacting pressure may be, for example, from about 100 to about 7000 kPa. The benzene to hydrogen molar ratio in the contacting step is preferably from about 0.01 to about 100. The WHSV during the contacting step is preferably in the range of about 0.01 to about 100.

The term “MCM-22 family material” (or “material of the MCM-22 family” or “molecular sieve of the MCM-22 family” or “MCM-22 family zeolite”), as used herein, includes one or more of:

- molecular sieves made from a common first degree crystalline building block unit cell, which unit cell has the MWW framework topology. (A unit cell is a spatial arrangement of atoms which if tiled in three-dimensional space describes the crystal structure. Such crystal structures are discussed in the “Atlas of Zeolite Framework Types”, Fifth edition, 2001, the entire content of which is incorporated as reference);
- molecular sieves made from a common second degree building block, being a 2-dimensional tiling of such MWW framework topology unit cells, forming a monolayer of one unit cell thickness, preferably one c-unit cell thickness;
- molecular sieves made from common second degree building blocks, being layers of one or more than one unit cell thickness, wherein the layer of more than one unit cell thickness is made from stacking, packing, or binding at least two monolayers of one unit cell thickness. The stacking of such second degree building blocks can be in a regular fashion, an irregular fashion, a random fashion, or any combination thereof; and
- molecular sieves made by any regular or random 2-dimensional or 3-dimensional combination of unit cells having the MWW framework topology.

Molecular sieves of the MCM-22 family include those molecular sieves having an X-ray diffraction pattern including d-spacing maxima at 12.4±0.25, 6.9±0.15, 3.57±0.07 and 3.42±0.07 Angstrom. The X-ray diffraction data used to characterize the material are obtained by standard techniques such as using the K-alpha doublet of copper as incident radiation and a diffractometer equipped with a scintillation counter and associated computer as the collection system.

Materials of the MCM-22 family include MCM-22 (described in U.S. Pat. No. 4,954,325), PSH-3 (described in U.S. Pat. No. 4,439,409), SSZ-25 (described in U.S. Pat. No. 4,826,667), ERB-1 (described in European Patent No. 0293032), ITQ-1 (described in U.S. Pat. No. 6,077,498), ITQ-2 (described in International Patent Publication No. WO 97/17290), MCM-36 (described in U.S. Pat. No. 5,250,277), MCM-49 (described in U.S. Pat. No. 5,236,575), MCM-56 (described in U.S. Pat. No. 5,362,697), UZM-8 (described in U.S. Pat. No. 6,756,030), and mixtures thereof. Molecular sieves of the MCM-22 family are preferred as the alkylation catalyst since they have been found to be highly selective to the production of sec-butylbenzene, as compared with the other butylbenzene isomers. Preferably, the molecular sieve is selected from (a) MCM-49, (b) MCM-56 and (c) isotypes of MCM-49 and MCM-56, such as ITQ-2.

Hydrocarbon Oxidation

The oxidation step in the present process is accomplished by contacting the hydrocarbon substrate with an oxygen-containing gas in the presence of a catalyst comprising a cyclic imide of the general formula (I):

wherein each of R¹and R²is independently selected from hydrocarbyl and substituted hydrocarbyl radicals having 1 to 20 carbon atoms, or the groups SO₃H, NH₂, OH and NO₂, or the atoms H, F, Cl, Br and I, provided that R¹and R²can be linked to one another via a covalent bond; each of Q¹and Q²is independently selected from C, CH, N and CR³; each of X and Z is independently selected from C, S, CH₂, N, P and elements of Group 4 of the Periodic Table; Y is O or OH; k is 0, 1, or 2; 1 is 0, 1, or 2; m is 1 to 3, and R³can be any of the entities (radicals, groups, or atoms) listed for R¹. Conveniently, each of R¹and R²is independently selected from aliphatic alkoxy or aromatic alkoxy radicals, carboxyl radicals, alkoxy-carbonyl radicals and hydrocarbon radicals, each of which radicals has 1 to 20 carbon atoms.

Generally, the cyclic imide employed as the oxidation catalyst obeys the general formula:

wherein each of R⁷, R⁸, R⁹, and R¹⁰is independently selected from hydrocarbyl and substituted hydrocarbyl radicals having 1 to 20 carbon atoms, or the groups SO₃H, NH₂, OH and NO₂, or the atoms H, F, Cl, Br and I; each of X and Z is independently selected from C, S, CH₂, N, P and elements of Group 4 of the Periodic Table; Y is O or OH; k is 0, 1, or 2, and 1 is 0, 1, or 2. Conveniently, each of R⁷, R⁸, R⁹, and R¹⁰is independently selected from aliphatic alkoxy or aromatic alkoxy radicals, carboxyl radicals, alkoxy-carbonyl radicals and hydrocarbon radicals, each of which radicals has 1 to 20 carbon atoms.

In one practical embodiment, the cyclic imide catalyst comprises N-hydroxyphthalimide (NHPI).

The conditions used to effect the oxidation step vary significantly with the type of hydrocarbon substrate to be oxidized, but generally suitable conditions include a temperature of between about 20° C. and about 150° C., such as between about 70° C. and about 130° C. The oxidation step is preferably carried out at a pressure between about 15 kPa and about 500 kPa, such as between 15 kPa to about 150 kPa.

Treatment of Oxidation Effluent

Depending on the nature of the hydrocarbon substrate, the product of the oxidation step may include one or more of a hydroperoxide, alcohol, ketone, carboxylic acid or dicarboxylic acid of the corresponding hydrocarbon. In addition, however, the effluent from the oxidation process may contain unreacted cyclic imide catalyst in addition to the desired hydrocarbon oxidation product. Thus, according to the present process, the oxidation effluent is treated with at least one solid sorbent, which is effective to remove some or substantially all of the unreacted imide catalyst, so as to produce a treated effluent which is rich in said oxidized hydrocarbon product and which contains a reduced or zero level of cyclic imide. Preferably, the sorption process is conducted so as to recover at least 80% of the imide in the organic phase, such as at least 90%, for example at least 99%. This is desirable not only because the imide is expensive but also because it can have deleterious effects on downstream operations and separations such as hydroperoxide cleavage.

Suitable solid sorbents are those having basic properties, including alkali metal carbonates, alkali metal bicarbonates, alkali metal hydroxides, alkali metal hydroxide-carbonate complexes, alkaline earth metal carbonates, alkaline earth metal bicarbonates, alkaline earth metal hydroxide-carbonate complexes, and preferably, alkaline earth metal hydroxides. In one embodiment, the at least one solid sorbent comprises an alkaline earth metal hydroxide, preferably calcium hydroxide (Ca(OH)₂), magnesium hydroxide (Mg(OH)₂) or a mixture thereof. Calcium hydroxide may be derived from the action of water on calcium oxide. Magnesium hydroxide may be derived by precipitation from a solution of magnesium salt by a base, such as sodium hydroxide.

In another embodiment, the alkali metal carbonates suitable for use as solid sorbents include sodium carbonate (Na₂CO₃) and potassium carbonate (K₂CO₃). The carbonates may be prepared using a variety of conventional techniques, and are generally are prepared by conversion of a suitable precursor by precipitation from a salt solution. Suitable precursors include metal salts, such as halides.

In another embodiment, the alkali metal bicarbonates suitable for use as solid sorbents include sodium bicarbonate (NaHCO₃) and potassium bicarbonate (KHCO₃). The alkali metal bicarbonates may be prepared using conventional techniques such as conversion of a suitable precursor by precipitation from solution. Suitable precursors include soda ash and potassium carbonate and water mixtures.

In another embodiment, the alkaline earth metal carbonates for use as solid sorbents include calcium carbonate (CaCO₃). Calcium carbonate occurs naturally, and may be derived by synthetic precipitation, such as reacting calcium chloride and sodium carbonate in water solution or passing carbon dioxide through a suspension of hydrated lime (Ca(OH)₂) in water.

In yet another embodiment, the alkaline earth metal hydroxide-carbonate complexes for use as solid sorbents include magnesium hydroxide-carbonate complexes such as artinite (MgCO₃.Mg(OH)₂.3H₂O), hydromagnestite (4MgCO₃.Mg(OH)₂.4H₂O), and dypingite (4MgCO₃.Mg(OH)₂.5H₂O). A magnesium hydroxide-carbonate complex generally refers to the various formulas for basic magnesium carbonates. Magnesium hydroxide-carbonate complexes may be derived by precipitation from a magnesium salt solution.

Various solid sorbents taught by the present invention are presented in Table I below with supplier information and general descriptions:

TABLE I

Example
No.	Solid Sorbent	Supplier	Description

1	Na₂CO₃	Sigma-Aldrich	99+%,
			Anhydrous
			powder
2	NaHCO₃	J. T. Baker	“Baker
			Analyzed”
			powder
3	K₂CO₃	Sigma-Aldrich	99+%,
			Granular,
			crushed
4	KHCO₃	J. T. Baker	Granular,
			crushed
5	CaCO₃	Sigma-Aldrich	99+%
6	(MgCO₃)₄Mg(OH)₂XH₂O	Sigma-Aldrich	99%
7	Ca(OH)₂	Sigma-Aldrich	95+%, powder
8	Mg(OH)₂	Sigma-Aldrich	95%, powder

The conditions used in the cyclic imide sorption step are not closely controlled but generally include a temperature of about 10° C. to about 130° C., such as about 20° C. to about 80° C. The time of sorption may be, for example, from about 1 minute to about 30 minutes, such as about 5 minutes to about 10 minutes.

After removal by the at least one solid sorbent, the unreacted cyclic imide can readily be recovered by washing the sorbent with a polar solvent, for example with ethanol or acetone or any acid e.g., acetic acid or hydrochloric acid. The recovered imide can then be recycled to the oxidation step, with or without prior removal of the ethanol, since it is found that the presence of ethanol with the imide does not adversely affect the oxidation activity or selectivity of the catalyst.

Oxidation Product

The product of the present oxidation process depends on the nature of the hydrocarbon substrate being oxidized but in general is a hydroperoxide, alcohol, ketone, carboxylic acid or dicarboxylic acid, especially a hydroperoxide.

For example, when the hydrocarbon substrate is isobutane, the oxidation product comprises tertiary butyl hydroperoxide (which is useful as an oxidizing agent e.g., for olefin epoxidation) and tertiary butanol (which is useful as a gasoline additive).

When the hydrocarbon substrate is cyclohexane, the oxidation product comprises cyclohexyl hydroperoxide, cyclohexanol and cyclohexanone. Cyclohexyl hydroperoxide is readily decomposed to additional cyclohexanol and cyclohexanone, either thermally or with the assistance of a catalyst. Cyclohexanol can be oxidized with aqueous nitric acid to produce adipic acid, which is a precursor in the synthesis of Nylon 6,6, whereas cyclohexanone can be converted to cyclohexanoxime which undergoes acid-catalyzed rearrangement to produce caprolactam, a precursor in the synthesis of Nylon 6.

Where the hydrocarbon substrate is an alkylaromatic compound of the general formula (II), the product of the oxidation reaction includes a hydroperoxide of general formula (IV):

in which R⁴, R⁵and R⁶have the same meaning as in formula (II). Preferably, the hydroperoxide is sec-butylbenzene hydroperoxide or cyclohexylbenzene hydroperoxide. This hydroperoxide can then be converted by acid cleavage to phenol or a substituted phenol and an aldehyde or ketone of the general formula R⁴COCH₂R⁵(V), in which R⁴and R⁵have the same meaning as in formula (II). Phenol can of course be reacted with acetone to produce bisphenol A, a precursor in the production of polycarbonates and epoxy resins.

The hydroperoxide cleavage reaction is conveniently effected by contacting the hydroperoxide with a catalyst in the liquid phase at a temperature of about 20° C. to about 150° C., such as about 40° C. to about 120° C., and/or a pressure of about 50 to about 2500 kPa, such as about 100 to about 1000 kPa and/or a liquid hourly space velocity (LHSV) based on the hydroperoxide of about 0.1 to about 100 hr⁻¹, preferably about 1 to about 50 hr⁻¹. The hydroperoxide is preferably diluted in an organic solvent inert to the cleavage reaction, such as methyl ethyl ketone, phenol or sec-butylbenzene, to assist in heat removal. The cleavage reaction is conveniently conducted in a catalytic distillation unit.

The catalyst employed in the cleavage step can be a homogeneous catalyst or a heterogeneous catalyst.

Suitable homogeneous cleavage catalysts include sulfuric acid, perchloric acid, phosphoric acid, hydrochloric acid and p-toluenesulfonic acid. Ferric chloride, boron trifluoride, sulfur dioxide and sulfur trioxide are also effective homogeneous cleavage catalysts. The preferred homogeneous cleavage catalyst is sulfuric acid.

A suitable heterogeneous catalyst for use in the cleavage of sec-butylbenzene hydroperoxide includes a smectite clay, such as an acidic montmorillonite silica-alumina clay, as described in U.S. Pat. No. 4,870,217 (Texaco), the entire disclosure of which is incorporated herein by reference.

The invention will now be more particularly described with reference to the following non-limiting Examples.

EXAMPLES

The present invention is more particularly described in the examples presented in Table II. These examples that are intended as illustrations only, since numerous modifications and variations within the scope of the present invention will be apparent to those skilled in the art. Unless otherwise noted, all parts and percentages reported in the following examples are on a weight basis, and all solid sorbents used in the examples were obtained, or are available, from the chemical suppliers described in Table I above, or may be synthesized by conventional techniques.

Table II below summarizes NHPI recovery of various example solid sorbents under constant conditions. “NHPI recovery,” which reflects the quantity of NHPI recovered after treatment with the solid sorbent, is defined by the general formula (V):

\begin{matrix} N H P I Recovery (%) = (100 % - \frac{(C_{o} - C_{1})}{C_{0}}) & (V) \end{matrix}

where,
C₀=Pre-treatment NHPI concentration (ppm)
C₁=Post-treatment NHPI concentration (ppm)

“Pre-treatment NHPI concentration” refers to the concentration of the NHPI in the product of the oxidation step prior to treatment with the solid sorbent. “Post-treatment NHPI concentration” refers to the NHPI in the same product of the oxidation after treatment with the solid sorbent.

In the examples of Table II, 1 gram of the respective solid sorbent was mixed with 5 milliliters of exemplary hydrocarbon oxidation product, cyclohexylbenzene-hydroperoxide (CHBHP). This mixture was further stirred at room temperature for a period of time. The data is summarized in Table 2 below:

	TABLE II

	NHPI (ppm)	NHPI

Exam-		before	after	Recov-
ple		treat-	treat-	ery	CHBHP
No.	Solid Sorbent	ment	ment	(%)	(wt. %)

1	Na₂CO₃	592	100	83%	21.4
2	NaHCO₃	769	474	38%	16.7
3	K₂CO₃	592	296	50%	20.7
4	KHCO₃	592	56	91%	21
5	CaCO₃	592	508	14%	21.4
6	(MgCO₃)₄Mg(OH)₂XH₂O	592	40	93%	21.2
7	Ca(OH)₂	769	<10	99%	16.2
8	Mg(OH)₂	769	<10	99%	16.1

While the present invention has been described and illustrated by reference to particular embodiments, those of ordinary skill in the art will appreciate that the invention lends itself to variations not necessarily illustrated herein. For this reason, then, reference should be made solely to the appended claims for purposes of determining the true scope of the present invention.

Claims

The invention claimed is:

1. A process for oxidizing a hydrocarbon to a corresponding hydroperoxide, alcohol, ketone, carboxylic acid or dicarboxylic acid, the process comprising:

wherein each of R¹and R²is independently chosen from hydrocarbyl and substituted hydrocarbyl radicals having 1 to 20 carbon atoms, or from the groups SO₃H, NH₂, OH and NO₂, or from the atoms H, F, Cl, Br and I, provided that R¹and R²can be linked to one another via a covalent bond;

each of Q¹and Q²is independently chosen from C, CH, N and CR³;

each of X and Z is independently chosen from C, S, CH₂, N, P and elements of Group 4 of the Periodic Table;

Y is O or OH;

k is 0, 1, or 2;

l is 0, 1, or 2;

m is 1 to 3; and

R³can be any of the entities listed for R¹; and

wherein said contacting produces an effluent comprising an oxidized hydrocarbon product and unreacted imide catalyst of said formula (I); and

(b) treating the effluent with at least one solid sorbent to remove at least part of said unreacted imide catalyst of said formula (I) from said effluent and produce a treated effluent comprising said oxidized hydrocarbon product, where said at least one solid sorbent is chosen from alkali metal carbonates, alkali metal bicarbonates, alkali metal hydroxides, alkali metal hydroxide-carbonate complexes, alkaline earth metal carbonates, alkaline earth metal bicarbonates, alkaline earth metal hydroxides, and alkaline earth metal hydroxide-carbonate complexes.

2. The process of claim 1, wherein said cyclic imide obeys the general formula (III):

wherein each of R⁷, R⁸, R⁹, and R¹⁰is independently chosen from hydrocarbyl and substituted hydrocarbyl radicals having 1 to 20 carbon atoms, or from the groups SO₃H, NH₂, OH and NO₂or from the atoms H, F, Cl, Br and I;

Y is O or OH,

k is 0, 1, or 2, and

l is 0, 1, or 2.

3. The process of claim 1, wherein the cyclic imide comprises N-hydroxyphthalimide.

4. The process of claim 1, wherein the contacting (a) is conducted at a temperature of between 20° C. and 150° C.

5. The process of claim 4, wherein the temperature is between 70° C. and 130° C.

6. The process of claim 1, wherein contacting (a) is conducted at a pressure between 15 kPa and 500 kPa.

7. The process of claim 6, wherein the pressure is from 15 kPa to 150 kPa.

8. The process of claim 1, wherein the at least one solid sorbent is chosen from alkali metal carbonates, alkali metal bicarbonates, and alkali metal hydroxide-carbonate complexes.

9. The process of claim 1, wherein the at least one solid sorbent is an alkaline metal carbonate.

10. The process of claim 9, wherein the alkaline metal carbonate is chosen from sodium carbonate (Na₂CO₃) and potassium carbonate (K₂CO₃).

11. The process of claim 9, wherein the alkaline metal carbonate is sodium carbonate (Na₂CO₃).

12. The process of claim 1, wherein the at least one solid sorbent is an alkaline metal bicarbonate.

13. The process of claim 12, wherein the alkaline metal bicarbonate is potassium bicarbonate (KHCO₃).

14. The process of claim 1, wherein the at least one solid sorbent is chosen from alkaline earth metal carbonates, alkaline earth metal bicarbonates, and alkaline metal hydroxide-carbonate complexes.

15. The process of claim 1, wherein the at least one solid sorbent is chosen from an alkaline metal hydroxide-carbonate complex.

16. The process of claim 15, wherein the alkaline metal hydroxide-carbonate complex is chosen from artinite (MgCO₃.Mg(OH)₂.3H₂O), hydromagnestite (4MgCO₃.Mg(OH)₂.4H₂O), and dypingite (4MgCO₃.Mg(OH)₂.5H₂O).

17. The process of claim 15, wherein the alkaline metal hydroxide-carbonate complex is artinite (MgCo₃.Mg(OH)₂.3H₂O).

18. The process of claim 1, wherein the at least one solid sorbent is an alkaline metal hydroxide.

19. The process of claim 18, wherein the alkaline metal hydroxide is chosen from calcium hydroxide (Ca(OH)₂) and magnesium hydroxide (Mg(OH)₂).

20. The process of claim 1, and further comprising recovering the unreacted imide catalyst removed by the at least one solid sorbent and recycling the catalyst to (a).

21. The process of claim 1, wherein the unreacted imide catalyst is recovered from the at least one solid sorbent by washing the at least one solid sorbent with a polar solvent.

22. The process of claim 1, wherein the hydrocarbon comprises an alkylaromatic compound of general formula (II):

wherein R⁴and R⁵each independently represents hydrogen or an alkyl group having from 1 to 4 carbon atoms, provided that R⁴and R⁵may be joined to form a cyclic group having from 4 to 10 carbon atoms, said cyclic group being optionally substituted, and R⁶represents hydrogen, one or more alkyl groups having from 1 to 4 carbon atoms or a cyclohexyl group, and wherein the oxidized hydrocarbon product comprises a hydroperoxide of general formula (IV):

in which R⁴, R⁵and R⁶have the same meaning as in formula (II).

23. The process of claim 22, wherein the alkylaromatic compound of general formula (II) is chosen from ethyl benzene, cumene, sec-butylbenzene, sec-pentylbenzene, p-methyl-sec-butylbenzene, 1,4-diphenylcyclohexane, sec-hexylbenzene, and cyclohexylbenzene.

24. The process of claim 22, wherein the alkylaromatic compound is sec-butylbenzene or cyclohexylbenzene.